饲料中添加水飞蓟素对鳜生长、糖脂代谢及抗氧化的影响

DIETARY SUPPLEMENTATION OF SILYMARIN ON GROWTH, GLYCOLIPID METABOLISM, AND ANTIOXIDANT ACTIVITY OF MANDARIN FISH (SINIPERCA CHUATSI)

  • 摘要: 实验探究使用水飞蓟素拌料投喂对鳜的生长状况、糖脂代谢及抗氧化性能的影响, 旨在探究适宜鳜的饲料添加剂。在商品饲料中分别添加0、0.5‰、2‰和3.5‰的水飞蓟素, 分别记为A0、A0.5、A2和A3.5组, 将健康的鳜360尾均重(35±0.69) g随机分为4组, 每组3个重复, 每个重复30尾, 分别投喂以上4种实验饲料, 饲养时间为69d。结果表明: (1)各组鳜增重率、特定生长率、肥满度、肝体比、肠系膜脂肪指数均无显著差异, A2、A3.5组饲料系数显著降低(P<0.05)。添加水飞蓟素的处理组鳜存活率显著高于A0组, A2组存活率达到最大(P<0.05)。(2)添加水飞蓟素的各组鳜血清甘油三酯、肝糖原浓度均显著降低(P<0.05), A3.5组达到最低。肌肉糖原在A2和A3.5组显著低于对照组(P<0.05)。添加水飞蓟素的各组鳜胰岛素、胰高血糖素浓度均显著升高(P<0.05), A3.5组达到最大(P<0.05)。(3)肝脏HE病理切片观察到添加水飞蓟素组鳜肝脏组织细胞空泡化减少、血窦堵塞、细胞核偏移现象缓解, 细胞核、细胞质结构及细胞边界相比A0组鳜更完整清晰。(4) A2和A3.5组葡萄糖激酶、磷酸烯醇式丙酮酸羧激酶酶活显著高于对照组(P<0.05), 添加水飞蓟素各组的磷酸果糖激酶1、丙酮酸激酶、果糖1,6-二磷酸酶酶活均显著降低(P<0.05)。添加水飞蓟素各组鳜肝脏总抗氧化能力显著提高(P<0.05)。(5)添加水飞蓟素后鳜肝糖原合成相关基因gys2 mRNA水平显著降低, 糖代谢相关基因中gkpfk1g6ppepck水平显著降低(P<0.05)。水飞蓟素添加组鳜肝脏中抗氧化相关基因catgpx mRNA水平显著高于对照组(P<0.05)。综上, 鳜饲料中添加水飞蓟素能够显著提高鳜存活率和饲料利用率, 调节鳜糖脂代谢、减少糖原沉积与脂质蓄积, 提升肝脏抗氧化能力。添加量为2‰、3.5‰时, 效果明显。

     

    Abstract: Silymarin was added to commercial feed at ratios of 0, 0.5‰, 2‰, and 3.5‰, designated as groups A0, A0.5, A2, and A3.5, respectively. A total of 360healthy mandarin fish (Siniperca chuatsi) with an average weight of (35±0.69) g were randomly divided into 4 groups, with 3 replicates in each group and 30 per replicate. The fish were fed the experimental diets for 69d. The results showed that: (1) There were no significant changes in weight gain rate, specific growth rate, plumpness, liver to body ratio, and mesenteric fat index in each group of mandarin fish (P>0.05), while the feed coefficient of A2 and A3.5 groups significantly decreased (P<0.05). The survival rate in the treatment group with the addition of silymarin was significantly higher than that in the A0 group, and the A2 group had the highest survival rate (P<0.05). (2) The content of liver and muscle glycogen significantly decreased with the increase of silymarin supplementation (P<0.05). The serum triglyceride concentration of each group with the addition of silymarin significantly decreased, reaching the lowest level in the A3.5 group (P<0.05). As the amount of silymarin added to the feed increased, the concentrations of insulin and glucagon (GCG) in the serum of each group gradually increased, reaching their maximum in the A3.5 group (P<0.05). (3) The H&E pathological sections also observed a decrease in cellular vacuolization, sinus blockage, and alleviation of nuclear translocation in the liver tissue treated with silymarin. The nuclear and cytoplasmic structures, as well as cell boundaries, were more complete and clearer compared to the A0 group. (4) The activities of glucose kinase and phosphoenolpyruvate carboxylase were significantly increased in groups A2 and A3.5 (P<0.05), and the activity of glucose-6-phosphatase (G6P) gradually increased with the increase of silymarin addition (P<0.05), while hexokinase activity significantly decreased in groups A2 and A3.5 (P<0.05). Activities of phosphofructose kinase 1 and pyruvate kinase in groups with silymarin addition were significantly reduced (P<0.05). The total antioxidant capacity of the liver significantly increased with the addition of silymarin levels (P<0.05). (5) After adding silymarin, the expression of the glycogen synthesis related gene gys2 in the liver were significantly reduced, while the levels of gk, pfk1, and g6p in glucose metabolism related genes were significantly reduced (P<0.05). The fas expression of lipid metabolism related genes in group A2 was significantly reduced (P<0.05), and lpl expression levels in A0.5 and A3.5 groups were significantly reduced (P<0.05). Compared with group A0, the level of antioxidant related gene cat expression in the liver increased with the increase of silymarin addition, reaching its maximum in group A3.5 (P<0.05). The gpx expression significantly increased, reaching its maximum in the A0.5 group (P<0.05). In summary, adding silymarin to the feed of mandarin fish can significantly improve its survival rate and feed utilization, regulate its glucose and lipid metabolism, reduce glycogen deposition and lipid accumulation, and enhance its liver antioxidant capacity. Optimal effects were observed with silymarin supplementation levels of 2‰ and 3.5‰.

     

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